I have sff files from 454 sequencing. How do I convert sff to fasta or fastq format?
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I've converted sff to fastq using sffinfo to generate the fasta and qual files. You can then combine them using the perl script on this page
Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc
to combine them into Sanger fastq. Your fasta and qual files should have the same basename for it to work.
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I am building a tool with graphical interface that will convert SFF to FASTQ and multifasta.Last edited by create.share; 06-03-2014, 01:11 AM.
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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07-01-2026, 11:43 AM -
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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